Low molecular weight acyl peroxycarbonic esters

ABSTRACT

LOW MOLECULAR WEIGHT (4-7 CARBON ATOMS) ACYL PEROXYCARBONIC ALIPHATIC ESTERS.

United States Patent 3,736,344 LOW MOLECULAR WEIGHT ACYL PEROXYCARBONIC ESTERS Roger N. Lewis, Pinole, and Ronald L. Friedman, San Rafael, Califi, assignors to Argus Chemical Corp., Brooklyn, N.Y.

No Drawing. Original application Dec. 26, 1967, Ser. No. 693,187, now Patent No. 3,585,232. Divided and this application Jan. 8, 1971, Ser. No. 105,130

Int. Cl. C07c 69/00 US. Cl. 260463 6 Claims ABSTRACT OF THE DISCLOSURE Low molecular weight (4-7 carbon atoms) acyl peroxycarbonic aliphatic esters.

This is a division of application Ser. No. 693,187, filed Dec. 26, 1967, now US. Pat. No. 3,585,232.

This invention relates to organic peroxide composi tions. More particularly, the invention relates to low molecular weight aliphatic acyl peroxycarbonic esters that are useful for initiating the polymerization of monomers such as vinyl chloride.

US. Pat. No. 3,108,093 describes the use of certain acyl peroxycarbonic esters for the initiation of polymerization reactions. The present invention is an improvement on those aspects of said patent by virtue of the discovery that low molecular weight acyl peroxycarbonic esters, i.e. those having from 4-7 carbon atoms, are superior polymerization initiators as compared with analogous but higher molecular weight esters such as those described in said patent.

It has been found that the new low molecular weight esters of this invention provide higher yields of polymer product under comparable conditions. At the same time the present materials perform their initiation function at a desirable rapid rate. While providing these advantages in utility, the present materials are quite stable, exhibiting longer half-lives than their higher molecular weight analogs. This stability is of significant commercial advantage in terms of shipping and storing of the compounds.

In general, the preferred group of compounds of this invention can be described as having the formula:

0 o R-Q-O O-iL-OR wherein R and R are the same or different acyclic aliphatic groups, provided that the sum of the carbon atoms in R and R is not more than 5.

Best results have thus far been observed where R in the above formula is a methyl group so that a preferred group of peroxides Within the present invention may be referred to as acetyl peroxycarbonic esters.

In addition to alkyl groups, either straight or branched chain, derivatives within the invention broadly includes all of the aliphatic variations permissible within the molecular weight limitation imposed by the fact that R and R collectively do not exceed 5 carbon atoms. Thus R and/ or R may contain diverse substituents such as the halogens as will be exemplified hereinafter, ether linkages, or hydroxyl groups. R and R may also contain ethylenic or acetylenic unsaturation.

Typical compounds included are:

The new compounds of this invention may conveniently be made by the reaction of a peroxycarboxylic acid with a halo formate in accordance with the following general reaction. The basic catalyst may be sodium hydroxide, sodium carbonate, sodium bicarbonate, pyridine or trimethyl amine for examples.

0 0 o o g I base 1]; g I I R OOH+ RO 01 R- -00- OR salt The chloroformate is most generally selected for purposes of this reaction.

The compounds are principally contemplated for use in the production of polymers from monomers containing vinyl groups and which are capable of being polymerized in the usual fashion with a peroxide initiator. Typical monomers include ethylene, styrene, ethyl methacrylate, vinyl acetate, and the like. Exceptional results have been observed with the polymerization of vinyl chloride in the manufacture of polyvinyl chloride.

The following examples illustrates the preparation of compounds within the scope of this invention.

Example 1.Acetyl peroxyisobutyl carbonate added simultaneously dropwise in 10-13 minutes at -10 to -2 C. The reaction mixture is well stirred during these additions. After the reaction mixture is stirred an additional two hours at l0 to 1 C., 25 ml. ether, a small amount of NaCl, and about 125 ml. ice water are added. After phase separation, the organic layer is washed once with 35 ml. ice water, twice with 35 ml. cold dilute H (pH 1), once again with 35 ml. ice H O, twice with 40 ml. cold dilute KOH 1%), and finally with two additional 35 ml. ice Water washes. The organic layer is dried with anhydrous Na SO filtered through anhydrous MgSO and concentrated under vacuum using an ice water bath. Product A.O. (active oxygen) analysis: Theory, 9.08; Found, 8.52, 93.75% pure; 71.1% yield. A second synthesis gave a product of 95.83% purity and a yield of 76.7%.

Utilizing the above procedure except for the substitution of appropriate haloformates and peracids, the following materials were prepared in the purities and yields listed:

1 DMP=Dimethyl phthalate.

To illustrate the superiority of the new compounds as vinyl polymerization initiators, a series of polymerizations of vinyl chloride were carried out with various initiators. The tests were conducted in a 6 /2 fluid oz. ordinary Coke bottle. 94.0 grams of frozen dispersing solution was added to each Coke bottle. The dispersing solution is a conventional media for conducting suspension polymerization of vinyl chloride and contains water and suspending agents. Each Coke bottle also received 0.00094 mole of peroxide catalyst or initiator and 50.0 grams of vinyl chloride monomer. Since the catalysts were added on a molar basis, diflerenees in molecular weights are discounted and equivalent results should be obtained unless there is a difference in the inherent properties and efliciency of the catalysts.

After the contents were added to the Coke bottles, they were capped, the contents almost melted, and the bottles placed in a rotating constant temperature bath at 40 C. for 6 hours. The bottles were then cooled and excess monomer vented. The polyvinyl chloride product was filtered, washed and dried.

The following table shows the catalysts employed and the results in terms of weight yield and percent yield of polyvinyl chloride relative to the starting amount of vinyl chloride monomer:

TABLE 11 Utility as an initiator for vinyl chloride Lauroyl peroxide was selected from comparison in the above test since this material is most prevalent and typical of catalysts now used for making polyvinyl chloride. All of the other initiators in the table are compounds within the present invention and their advantage is dramatically shown in terms of increased yield of the desired polymer compared with the standard lauroyl peroxide.

This increased yield is obtained at a significantly increased rate. The following table lists data showing the relative conversion rates of an initiator within this invention (acetyl peroxy isobutyl carbonate) as compared with the standard lauroyl peroxide used in the polyvinyl chloride industry. The data were obtained during the execution of a vinyl chloride polymerization within a Coke bottle as described above. In this case the two initiators being compared were 0.25% by weight of the monomer.

TAB LE III [PVC conversion rate versus time, 30 0.]

Percent weight PVC yield, in time of- The unexpected superiority of the present materials as compared with analogous materials differing only by the presence of more than 7 carbon atoms in the molecule is demonstrated in this example. Here a composition provided by this invention (acetyl peroxy isobutyl carbonate) is compared with atypical higher molecular weight compound of the prior art (lauroyl peroxy isobutyl carbonate). These two initiators were used for the polymerization of vinyl chloride to produce polyvinyl chloride within a Coke bottle in the manner above described. In this case each of the initiators was added in an amount of 0.00050 mole of initiator to 50 grams of vinyl mono- 4 mer. The test was executed for 6 hours at 4012 C. The observed results are as follows:

TABLE IV Percent i t? me we Initiator grams avg:

1 Acct l erox isobut lcarbonate:

l t um 24.2-25.6 49.8 2d run 23. 0-23 4 46.4 2 Lauroyl peroxy isobutyl carbonat 1st run 13. 6-13.! 27. 3 2d run 13. 6-13. 6 27. 3

TABLE V Temperature, G.

Initiator 45 60 1 Acetyl peroxy isobutyl carbonate 33. 0 3.8 0. 5 2 Lauoyl peroxy isobutyl carbonate.-- 27. 0 3. 2 0. 4

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is understood that certain changes and modifications may be practiced within the spirit of the invention as limited only by the scope of the appended claims.

What is claimed is:

1. Acyl peroxycarbonic esters of the formula:

wherein R and R are the same or different acyclic aliphatic groups containing only members selected from carbon, hydrogen, halogen, hydroxyl, and alkoxy provided that the sum of the carbon atoms in R and R is not more than 5, and at least one of R and R contains a halogen atom, hydroxyl group, or alkoxy group.

2. An acyl peroxycarbonic ester in accordance with claim 1 wherein Ris a methyl group.

3. An acyl peroxycarbonic ester in accordance with claim 1 wherein said ester is acetyl peroxy Z-chloro ethyl carbonate.

4. An acyl peroxycarbonic ester in accordance with claim 1 wherein at least one of R and R contains a halogen atom.

5. An acyl peroxycarbonic ester in accordance with claim 1 wherein R is alkyl and R is halo-alkyl.

6. An acyl peroxycarbonic ester in accordance with claim 2 wherein R contains only carbon, hydrogen, and chlorine.

References Cited UNITED STATES PATENTS 3,108,093 10/1963 Pajaczkowski 260-895 LEWIS GOIT S, Primary Examiner D. G. RIVERS, Assistant Examiner 

